Chemical Formula: C9H12N2O4

Chemical Formula C9H12N2O4

Found 30 metabolite its formula value is C9H12N2O4

2',3'-Dideoxyuridine

1-[5-(hydroxymethyl)oxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione

C9H12N2O4 (212.07970319999998)


   

(1R,2R)-2-Amino-1-(4-nitrophenyl)propane-1,3-diol

1-(4-Nitrophenyl)-2-aminopropane-1,3-diol, (S)-hydroxybutanedioate (2:1) (S-(r*,r*))-isomer

C9H12N2O4 (212.07970319999998)


   
   

surugapyrrole A

surugapyrrole A

C9H12N2O4 (212.07970319999998)


A pyrrolecarboxamide obtained by the formal condensation of 1-hydroxy-4-methyl-1H-pyrrole-2-carboxylic acid with the amino group of 3-aminopropanoic acid. It is isolated from the culture broth of Streptomyces sp.USF-6280 and exhibits DPPH radical scavenging activity.

   

2,3-Dideoxyuridine

2,3-Dideoxyuridine

C9H12N2O4 (212.07970319999998)


D009676 - Noxae > D000963 - Antimetabolites > D015224 - Dideoxynucleosides

   

4-Hydroxy-3,5-dimethoxybenzoic acid

4-Hydroxy-3,5-dimethoxybenzoic acid

C9H12N2O4 (212.07970319999998)


   

Levoamine (Chloramphenicol D base)

(1R,2R)-2-Amino-1-(4-nitrophenyl)propane-1,3-diol

C9H12N2O4 (212.07970319999998)


   

METHYL 5,6-DIHYDROXY-2-ISOPROPYLPYRIMIDINE-4-CARBOXYLATE

METHYL 5,6-DIHYDROXY-2-ISOPROPYLPYRIMIDINE-4-CARBOXYLATE

C9H12N2O4 (212.07970319999998)


   

4-((3-Hydroxypropyl)amino)-3-nitrophenol

4-((3-Hydroxypropyl)amino)-3-nitrophenol

C9H12N2O4 (212.07970319999998)


   

1-(p-nitrophenyl)-2-amino-1,3-propanediol

1-(p-nitrophenyl)-2-amino-1,3-propanediol

C9H12N2O4 (212.07970319999998)


   

Methyl Ester L-Lysine Diisocyanate

Methyl Ester L-Lysine Diisocyanate

C9H12N2O4 (212.07970319999998)


   

(2,4-DICHLORO-PHENYL)-ACETYLCHLORIDE

(2,4-DICHLORO-PHENYL)-ACETYLCHLORIDE

C9H12N2O4 (212.07970319999998)


   

Ethyl 4,6-dimethoxypyrimidine-2-carboxylate

Ethyl 4,6-dimethoxypyrimidine-2-carboxylate

C9H12N2O4 (212.07970319999998)


   

3,5-Pyrazoledicarboxylic acid diethyl ester

3,5-Pyrazoledicarboxylic acid diethyl ester

C9H12N2O4 (212.07970319999998)


   

2-(5-methoxy-2-nitroanilino)ethanol

2-(5-methoxy-2-nitroanilino)ethanol

C9H12N2O4 (212.07970319999998)


   

2-[3-(methylamino)-4-nitrophenoxy]ethanol

2-[3-(methylamino)-4-nitrophenoxy]ethanol

C9H12N2O4 (212.07970319999998)


   
   

Pyridine,3,5-diethoxy-2-nitro-(9CI)

Pyridine,3,5-diethoxy-2-nitro-(9CI)

C9H12N2O4 (212.07970319999998)


   

Diethyl 1H-imidazole-4,5-dicarboxylate

Diethyl 1H-imidazole-4,5-dicarboxylate

C9H12N2O4 (212.07970319999998)


   

DIMETHYL 1-AMINO-3-METHYL-1H-PYRROLE-2,4-DICARBOXYLATE

DIMETHYL 1-AMINO-3-METHYL-1H-PYRROLE-2,4-DICARBOXYLATE

C9H12N2O4 (212.07970319999998)


   

Diethyl 3-amino-1H-pyrrole-2,4-dicarboxylate

Diethyl 3-amino-1H-pyrrole-2,4-dicarboxylate

C9H12N2O4 (212.07970319999998)


   

Benzoic acid,4-hydroxy-3,5-dimethoxy-, hydrazide

Benzoic acid,4-hydroxy-3,5-dimethoxy-, hydrazide

C9H12N2O4 (212.07970319999998)


   

2-NITRO-N-HYDROXYETHYL-p-ANISIDINE

2-NITRO-N-HYDROXYETHYL-p-ANISIDINE

C9H12N2O4 (212.07970319999998)


   

3-(4,6-dimethoxypyrimidin-2-yl)propanoicacid

3-(4,6-dimethoxypyrimidin-2-yl)propanoicacid

C9H12N2O4 (212.07970319999998)


   
   
   

2-((4-Methoxy-3-nitrophenyl)amino)ethanol

2-((4-Methoxy-3-nitrophenyl)amino)ethanol

C9H12N2O4 (212.07970319999998)


   

(1R,2R)-2-Amino-1-(4-nitrophenyl)propane-1,3-diol

(1R,2R)-2-Amino-1-(4-nitrophenyl)propane-1,3-diol

C9H12N2O4 (212.07970319999998)


   
   

2',3'-Dideoxyuridine

2',3'-Dideoxyuridine

C9H12N2O4 (212.07970319999998)


2',3'-Dideoxyuridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].